Qc Analyst – Sdms

Johnson & Johnson Johnson & Johnson · Pharma · Wilson, NC +1

The QC Analyst role at Johnson & Johnson's Biotherapeutics Manufacturing facility focuses on laboratory equipment lifecycle management, CSV support, and maintaining lab systems like SDMS, eLIMS/iLABS, Empower, and SoftMax Pro. Responsibilities include participating in the qualification of analytical equipment (HPLC, Spectrophotometry, etc.), authoring SOPs, and resolving compliance or instrument issues. The role requires a Bachelor's Degree in a science-related field with 2+ years of experience in the biopharmaceutical industry, working knowledge of regulatory requirements (cGMP, FDA/EU guidance), and strong technical knowledge of QC analytical equipment.

What you'd actually do

  1. Participate in activities to introduce and sustain laboratory technologies and computerized systems at a new site, with emphasis on SDMS (e.g., instrument data capture/integration, data integrity/ALCOA+ controls, template/report configuration, and migration/archiving), as well as eLIMS/iLABS, Empower and SoftMax Pro, to improve laboratory efficiency and promote a culture of Innovation.
  2. Participate in the qualification of analytical equipment for related testing functions, for example, IQ/OQ/PQ of HPLC, Spectrophotometry, Endotoxin, Cell Culture and Total Organic Carbon equipment.
  3. Author SOP’s, Work Instructions and protocols.
  4. Interact with the QC Global organization for the different center of excellence for equipment and information technologies.
  5. The resolution of unexpected complex compliance or lab instrument and system issues as they arise

Skills

Required

  • Bachelor’s Degree in Chemistry, Biochemistry, Micro or science related field with 2+ years related experience in biopharmaceutical or pharmaceutical industry.
  • Working knowledge of regulatory requirements, policies and guidelines.
  • Experience with Quality Control document reviews and regulatory inspection processes.
  • Working knowledge of laboratory systems.
  • Strong technical knowledge in and experience with QC analytical equipment.
  • Knowledge of cGMP regulations and FDA/EU guidance.

Nice to have

  • An unquestionable level of integrity and commitment to operating ethically and within the boundaries of regulatory requirements.
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and communicate complex quality concepts to stakeholders at all levels.
  • Proven ability to manage multiple priorities and work independently with minimal supervision.
  • Detail-oriented mindset, with a keen eye for identifying opportunities for process improvements.
  • Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment.
  • The ability to work in a team environment and interact with all levels of the organization.

What the JD emphasized

  • Working knowledge of regulatory requirements, policies and guidelines.
  • Knowledge of cGMP regulations and FDA/EU guidance is required.